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	<title>Pulmonary Fibrosis News Forums | Edward Grant | Activity</title>
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				<title>Edward Grant replied to the discussion Life span in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/life-span/#post-27928</link>
				<pubDate>Wed, 31 Mar 2021 11:46:04 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/life-span/page/2/#post-27928"><span class="bb-reply-lable">Reply to</span> Life span</a></p> <div class="bb-content-inr-wrap"><p>I lost my husband, my soulmate last week to a combination of heart failure and PF. I am posting to actually let those with this horrible disease know that the lifespan is variable and not written in stone. My husband was diagnosed over 20 years ago when a heart attack revealed the crackling in his lungs.  We had an amazing life and shared&hellip;<span class="activity-read-more" id="activity-read-more-26437"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/life-span/#post-27928" rel="nofollow"> Read more</a></span></p>
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				<title>Edward Grant replied to the discussion Dizziness and IPF in the forum PF Life: 50+</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/dizziness-and-ipf/#post-26762</link>
				<pubDate>Tue, 05 Jan 2021 21:49:05 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/dizziness-and-ipf/#post-26762"><span class="bb-reply-lable">Reply to</span> Dizziness and IPF</a></p> <div class="bb-content-inr-wrap"><p>I have experienced dizziness in the morning but thought it was from getting up too fast (well not too fast lol)! I use a nebulizer usually twice a day and find it helps get the mucus up. However the medicine makes me extremely shaky in not only my hands but my stomach also.  My nebulizer and oxygen attaches to a Volara machine by hillrom&hellip;<span class="activity-read-more" id="activity-read-more-24741"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/dizziness-and-ipf/#post-26762" rel="nofollow"> Read more</a></span></p>
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				<title>Edward Grant replied to the discussion DEALING WITH OFEV side effects in the forum PF Life: 50+</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/dealing-with-ofev-side-effects/#post-25856</link>
				<pubDate>Mon, 19 Oct 2020 23:24:21 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/dealing-with-ofev-side-effects/#post-25856"><span class="bb-reply-lable">Reply to</span> DEALING WITH OFEV side effects</a></p> <div class="bb-content-inr-wrap"><p>Thank you for your input. We appreciate the help.  Ed’s pulmonologist just put him on the 100mg instead of the 150mg. His main issue from the OFEV is the stomach pain.  He is on 2ml oxygen, takes pentoprazole for GERD and 5mg prednisone.  We have also found that taking small bites when eating ,careful swallowing, and no talking helps a little&hellip;<span class="activity-read-more" id="activity-read-more-23001"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/dealing-with-ofev-side-effects/#post-25856" rel="nofollow"> Read more</a></span></p>
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				<title>Edward Grant replied to the discussion DEALING WITH OFEV side effects in the forum PF Life: 50+</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/dealing-with-ofev-side-effects/#post-25844</link>
				<pubDate>Sun, 18 Oct 2020 16:27:53 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/dealing-with-ofev-side-effects/#post-25844"><span class="bb-reply-lable">Reply to</span> DEALING WITH OFEV side effects</a></p> <div class="bb-content-inr-wrap"><p>My husband just switched from Esbriet to OFEV.  He had the stomach pain with the Esbriet and now experiencing it with OFEV.   Rachel mentioned something about taking the Bio-K + probiotic.  Right now Ed is taking another nondairy probiotic drink. Our questions are how much should he take, should he take it everyday and should he take it with&hellip;<span class="activity-read-more" id="activity-read-more-22981"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/dealing-with-ofev-side-effects/#post-25844" rel="nofollow"> Read more</a></span></p>
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				<title>Edward Grant posted a new activity comment</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/18342/#acomment-18385</link>
				<pubDate>Sat, 29 Feb 2020 17:22:51 -0600</pubDate>

									<content:encoded><![CDATA[<p>Hi! I have been following the PF news for awhile but just  registered.  I not only find the site informative but it makes me feel not alone  in my struggles with PF. I am retired military and a Vietnam Vet. I was in Vietnam when Agent Orange was sprayed.  I have been on Esbriet for about 5 months but because of stomach issues I have stayed on&hellip;<span class="activity-read-more" id="activity-read-more-18385"><a href="https://pulmonaryfibrosisnews.com/forums/activity/p/18342/#acomment-18385" rel="nofollow"> Read more</a></span></p>
				<strong>In reply to</strong> -
					<a href="https://pulmonaryfibrosisnews.com/forums/members/edot/" data-bb-hp-profile="4657" rel="nofollow">Edward Grant</a> became a registered member					]]></content:encoded>
				
				
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				<title>Edward Grant became a registered member</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/18342/</link>
				<pubDate>Thu, 27 Feb 2020 18:06:05 -0600</pubDate>

				
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